Canonical Allele Identifier: CA384387022

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703436A>C (hg19) ; chr12:g.39309634A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309634A>C , CM000674.2:g.39309634A>C	GRCh38
NC_000012.11:g.39703436A>C , CM000674.1:g.39703436A>C	GRCh37
NC_000012.10:g.37989703A>C	NCBI36
NG_017067.1:g.138757T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4229T>G MANE Select	ENSP00000354878.5:p.Ile1410Ser
ENST00000636569.1:c.4166T>G	ENSP00000490369.1:p.Ile1389Ser
ENST00000361418.9:c.4229T>G	ENSP00000354878.5:p.Ile1410Ser
ENST00000361961.7:c.4190T>G	ENSP00000354851.3:p.Ile1397Ser
ENST00000541463.6:c.4070T>G	ENSP00000438075.2:p.Ile1357Ser
ENST00000544797.6:c.4118T>G	ENSP00000445606.2:p.Ile1373Ser
ENST00000547733.1:n.1543T>G
ENST00000551264.5:c.1172T>G	ENSP00000448792.1:p.Ile391Ser
ENST00000552961.5:c.2131T>G
NM_001173463.1:c.4118T>G	NP_001166934.1:p.Ile1373Ser
NM_001173464.1:c.4229T>G	NP_001166935.1:p.Ile1410Ser
NM_001173465.1:c.4070T>G	NP_001166936.1:p.Ile1357Ser
NM_017641.3:c.4190T>G	NP_060111.2:p.Ile1397Ser
XM_005269007.1:c.4232T>G	XP_005269064.1:p.Ile1411Ser
XM_005269008.1:c.4217T>G	XP_005269065.1:p.Ile1406Ser
XM_005269009.1:c.4211T>G	XP_005269066.1:p.Ile1404Ser
XM_005269010.1:c.4193T>G	XP_005269067.1:p.Ile1398Ser
XM_005269011.1:c.4178T>G	XP_005269068.1:p.Ile1393Ser
XM_005269012.1:c.4103T>G	XP_005269069.1:p.Ile1368Ser
XM_005269013.1:c.4088T>G	XP_005269070.1:p.Ile1363Ser
XM_005269014.1:c.4049T>G	XP_005269071.1:p.Ile1350Ser
XM_006719493.1:c.4172T>G	XP_006719556.1:p.Ile1391Ser
XM_006719494.1:c.4100T>G	XP_006719557.1:p.Ile1367Ser
XM_006719496.1:c.4157T>G	XP_006719559.1:p.Ile1386Ser
XM_011538556.1:c.4163T>G	XP_011536858.1:p.Ile1388Ser
XM_005269007.3:c.4232T>G	XP_005269064.1:p.Ile1411Ser
XM_005269008.3:c.4217T>G	XP_005269065.1:p.Ile1406Ser
XM_005269009.3:c.4211T>G	XP_005269066.1:p.Ile1404Ser
XM_005269010.3:c.4193T>G	XP_005269067.1:p.Ile1398Ser
XM_005269011.3:c.4178T>G	XP_005269068.1:p.Ile1393Ser
XM_005269012.3:c.4103T>G	XP_005269069.1:p.Ile1368Ser
XM_005269013.3:c.4088T>G	XP_005269070.1:p.Ile1363Ser
XM_005269014.3:c.4049T>G	XP_005269071.1:p.Ile1350Ser
XM_006719493.3:c.4172T>G	XP_006719556.1:p.Ile1391Ser
XM_006719494.3:c.4100T>G	XP_006719557.1:p.Ile1367Ser
XM_011538556.3:c.4163T>G	XP_011536858.1:p.Ile1388Ser
XM_017019607.2:c.4178T>G	XP_016875096.1:p.Ile1393Ser
XM_017019608.2:c.4139T>G	XP_016875097.1:p.Ile1380Ser
XM_017019609.2:c.4028T>G	XP_016875098.1:p.Ile1343Ser
XM_017019610.2:c.4028T>G	XP_016875099.1:p.Ile1343Ser
XM_017019611.2:c.4010T>G	XP_016875100.1:p.Ile1337Ser
NM_001173463.2:c.4118T>G	NP_001166934.1:p.Ile1373Ser
NM_001173464.2:c.4229T>G MANE Select	NP_001166935.1:p.Ile1410Ser
NM_001173465.2:c.4070T>G	NP_001166936.1:p.Ile1357Ser
NM_017641.4:c.4190T>G	NP_060111.2:p.Ile1397Ser
NM_001378439.1:c.4232T>G	NP_001365368.1:p.Ile1411Ser
NM_001378440.1:c.4217T>G	NP_001365369.1:p.Ile1406Ser
NM_001378441.1:c.4193T>G	NP_001365370.1:p.Ile1398Ser